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FDA 510(k)

TELET-LEX MEDICAL IV CATHETER PLACEMENT

K-Number: K851142 · 1985-07-05

ApplicantTeleflexmedical, Inc.
Decision Date1985-07-05
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TELET-LEX MEDICAL IV CATHETER PLACEMENT is the device name listed in this FDA 510(k) record. The listed applicant is Teleflexmedical, Inc.. It received FDA 510(k) clearance on 1985-07-05 under 510(k) number K851142. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TELET-LEX MEDICAL IV CATHETER PLACEMENT?

TELET-LEX MEDICAL IV CATHETER PLACEMENT is a medical device that received FDA 510(k) clearance on 1985-07-05. The listed applicant is Teleflexmedical, Inc.. The 510(k) number is K851142.

When did TELET-LEX MEDICAL IV CATHETER PLACEMENT receive FDA 510(k) clearance?

TELET-LEX MEDICAL IV CATHETER PLACEMENT received FDA 510(k) clearance on 1985-07-05, under 510(k) number K851142.

Who is the listed applicant for TELET-LEX MEDICAL IV CATHETER PLACEMENT?

The FDA 510(k) record lists Teleflexmedical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TELET-LEX MEDICAL IV CATHETER PLACEMENT?

The FDA product code for TELET-LEX MEDICAL IV CATHETER PLACEMENT is FOZ.

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Related Devices (Code: FOZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260432Ruby Intravascular CatheterVenocare, Inc.K260165Unimpregnated Central Venous CatheterSpectrum VascularK261041ClearSafe Closed SystemMedSource Labs, LLCK260539MedSource QuickSafe™ Safety IV Catheter; MedSource PurSafe™ Safety IV CatheterMedSource Labs, LLCK253235Introcan Safety® Deep Access XL IV CatheterB.Braun Medical, Inc.K252137BD Insyte™ IV CatheterBecton Dickinson Infusion Therapy Systems, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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